First published online November 14, 2002; 10.1104/pp.009969
Plant Physiol, December 2002, Vol. 130, pp. 1706-1716
Expressed Sequence Tag-Based Gene Expression Analysis under
Aluminum Stress in Rye1,[w]
Miguel A. Rodriguez
Milla,
Ed
Butler,2
Alicia
Rodriguez
Huete,
Cindy F.
Wilson,
Olin
Anderson, and
J. Perry
Gustafson*
Departments of Agronomy (M.A.R.M., J.P.G.), and Biochemistry
(A.R.H.), and United States Department of Agriculture-Agricultural
Research Service, Plant Genetics Research Unit (J.P.G.), University of
Missouri, Columbia, Missouri 65211; Genetic Resources Conservation
Program, University of California, Davis, California 95616 (E.B.,
C.F.W.); and United States Department of Agriculture-Agricultural
Research Service, Pacific West Area, Western Regional Research Center,
Albany, California 94710 (O.A.)
To understand the mechanisms responsible for aluminum (Al) toxicity
and tolerance in plants, an expressed sequence tag (EST) approach was
used to analyze changes in gene expression in roots of rye
(Secale cereale L. cv Blanco) under Al stress. Two cDNA libraries were constructed (Al stressed and unstressed), and a total of
1,194 and 774 ESTs were generated, respectively. The putative proteins
encoded by these cDNAs were uncovered by Basic Local Alignment Search
Tool searches, and those ESTs showing similarity to proteins of known
function were classified according to 13 different functional
categories. A total of 671 known function genes were used to analyze
the gene expression patterns in rye cv Blanco root tips under Al
stress. Many of the previously identified Al-responsive genes showed
expression differences between the libraries within 6 h of Al
stress. Certain genes were selected, and their expression profiles were
studied during a 48-h period using northern analysis. A total of 13 novel genes involved in cell elongation and division (tonoplast
aquaporin and ubiquitin-like protein SMT3), oxidative stress
(glutathione peroxidase, glucose-6-phosphate-dehydrogenase, and
ascorbate peroxidase), iron metabolism (iron deficiency-specific proteins IDS3a, IDS3b, and IDS1; S-adenosyl methionine
synthase; and methionine synthase), and other cellular mechanisms
(pathogenesis-related protein 1.2, heme oxygenase, and epoxide
hydrolase) were demonstrated to be regulated by Al stress. These genes
provide new insights about the response of Al-tolerant plants to toxic
levels of Al.
1
This work was supported in part by the National
Science Foundation (grant no. 9975989) and by the Instituto Nacional de
Investigacion y Tecnologia Agraria y Alimentaria, Spain (scholarship to
M.A.R.M.). This is a contribution from the U.S. Department of
Agriculture, Agricultural Research Service, Plant Genetics Research
Unit, and the University of Missouri Agricultural Experiment Station.
Mention of a proprietary product does not constitute an endorsement or a recommendation for its use by the U.S. Department of
Agriculture-Agricultural Research Service or the University of Missouri.
2
Present address: Department of Plant Sciences,
University of Arizona, Tucson, AZ 85721.
[w]
The online version of this article contains Web-only
data. The supplemental material is available at www.plantphysiol.org.
*
Corresponding author; e-mail pgus{at}missouri.edu; fax 573-875-5359.
© 2002 American Society of Plant Biologists
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